Chr Mutation (hg38) CAid Gene Transcript Linkouts
7g.128845235G>ACA369198002FLNCc.3770G>A (p.Gly1257Glu)
7g.128845235G>CCA369198000FLNCc.3770G>C (p.Gly1257Ala)
7g.128845235G>TCA369197999FLNCc.3770G>T (p.Gly1257Val)
7g.128845236G>ACA4475119FLNCc.3771G>A (p.Gly1257=)
dbSNP ExAC gnomAD v2 gnomAD v4
7g.128845236G>CCA457579385FLNCc.3771G>C (p.Gly1257=)
7g.128845236G=CA1742585452FLNCc.3771G= (p.Gly1257=)
7g.128845236G>TCA457579388FLNCc.3771G>T (p.Gly1257=)
7g.128845237C>ACA369198012FLNCc.3772C>A (p.Pro1258Thr)
dbSNP gnomAD v3 gnomAD v4
7g.128845237C=CA1742585460FLNCc.3772C= (p.Pro1258=)
7g.128845237C>GCA369198014FLNCc.3772C>G (p.Pro1258Ala)
7g.128845237C>TCA4475120FLNCc.3772C>T (p.Pro1258Ser)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.128845238C>ACA369198020FLNCc.3773C>A (p.Pro1258His)
7g.128845238C=CA1742585461FLNCc.3773C= (p.Pro1258=)
7g.128845238C>GCA369198022FLNCc.3773C>G (p.Pro1258Arg)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
7g.128845238C>TCA369198025FLNCc.3773C>T (p.Pro1258Leu)
gnomAD v4
7g.128845239T>ACA457579403FLNCc.3774T>A (p.Pro1258=)
gnomAD v4
7g.128845239T>CCA457579407FLNCc.3774T>C (p.Pro1258=)
7g.128845239T>GCA457579405FLNCc.3774T>G (p.Pro1258=)
7g.128845240G>ACA369198028FLNCc.3775G>A (p.Gly1259Ser)
7g.128845240G>CCA369198031FLNCc.3775G>C (p.Gly1259Arg)
7g.128845240G>TCA369198033FLNCc.3775G>T (p.Gly1259Cys)
7g.128845241G>ACA369198036FLNCc.3776G>A (p.Gly1259Asp)
ClinVar
7g.128845241G>CCA369198039FLNCc.3776G>C (p.Gly1259Ala)
7g.128845241G>TCA369198042FLNCc.3776G>T (p.Gly1259Val)
7g.128845242T>ACA457579412FLNCc.3777T>A (p.Gly1259=)
7g.128845242T>CCA457579414FLNCc.3777T>C (p.Gly1259=)
7g.128845242T>GCA457579417FLNCc.3777T>G (p.Gly1259=)
7g.128845243G>ACA4475121FLNCc.3778G>A (p.Val1260Ile)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
7g.128845243G>CCA369198046FLNCc.3778G>C (p.Val1260Leu)
7g.128845243G=CA1742585465FLNCc.3778G= (p.Val1260=)
7g.128845243G>TCA369198047FLNCc.3778G>T (p.Val1260Phe)
7g.128845244T>ACA369198052FLNCc.3779T>A (p.Val1260Asp)
7g.128845244T>CCA369198056FLNCc.3779T>C (p.Val1260Ala)
7g.128845244T>GCA369198058FLNCc.3779T>G (p.Val1260Gly)
7g.128845245T>ACA457579428FLNCc.3780T>A (p.Val1260=)
7g.128845245T>CCA457579429FLNCc.3780T>C (p.Val1260=)
7g.128845245T>GCA457579431FLNCc.3780T>G (p.Val1260=)
7g.128845246G>ACA4475122FLNCc.3781G>A (p.Glu1261Lys)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
7g.128845246G>CCA369198063FLNCc.3781G>C (p.Glu1261Gln)
ClinVar dbSNP gnomAD v4
7g.128845246G=CA1742585470FLNCc.3781G= (p.Glu1261=)
7g.128845246G>TCA369198066FLNCc.3781G>T (p.Glu1261Ter)
7g.128845247A>CCA369198068FLNCc.3782A>C (p.Glu1261Ala)
7g.128845247A>GCA369198071FLNCc.3782A>G (p.Glu1261Gly)
7g.128845247A>TCA369198074FLNCc.3782A>T (p.Glu1261Val)
7g.128845248G>ACA457579449FLNCc.3783G>A (p.Glu1261=)
ClinVar dbSNP
7g.128845248G>CCA369198079FLNCc.3783G>C (p.Glu1261Asp)
7g.128845248G=CA1742585480FLNCc.3783G= (p.Glu1261=)
7g.128845248G>TCA369198082FLNCc.3783G>T (p.Glu1261Asp)
7g.128845249C>ACA369198092FLNCc.3784C>A (p.Pro1262Thr)
7g.128845249C>GCA369198089FLNCc.3784C>G (p.Pro1262Ala)

Number of alleles fetched